Year-end Sale % OFF 
Abstract
AbstractSince flavonoids exhibit a remarkable number of pharmacological properties like antioxidant, anti-inflammatory, and antimicrobial activities, a great deal of work has been done on the medicinal and therapeutical application of these compounds. Despite the central role of flavan-3,4-diols in the synthesis of many other classes of flavonoids, only a few methods for the preparation of these compounds have been reported. In this paper, the results on the preparation of methoxy-substituted flavan-3,4-diols, displaying natural substitution patterns, from readily available starting materials through a 3-step process is disclosed. It is also indicated that the 4-aryl-substituted analogues can become available from the corresponding flav-3-enes if an aromatic nucleophile is added during the dimethyldioxirane (DMDO) epoxidation process.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
